Canonical Allele Identifier: CA1479840960
Gene: ADH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99078208_99078210delinsTAG , CM000666.2:g.99078208_99078210delinsTAG GRCh38
NC_000004.11:g.99999359_99999361delinsTAG , CM000666.1:g.99999359_99999361delinsTAG GRCh37
NC_000004.10:g.100218382_100218384delinsTAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296412.14:c.345-1287_345-1285delinsCTA MANE Select ENSP00000296412.8:n.345-1287_345-1285delinsCTA
ENST00000296412.13:c.345-1287_345-1285delinsCTA ENSP00000296412.8:n.345-1287_345-1285delinsCTA
ENST00000296412.12:c.345-1287_345-1285delinsCTA ENSP00000296412.8:n.345-1287_345-1285delinsCTA
ENST00000502590.5:c.*25-1287_*25-1285delinsCTA ENSP00000422119.1:n.*25-1287_*25-1285delinsCTA
ENST00000503130.5:c.306-1287_306-1285delinsCTA ENSP00000427049.1:n.306-1287_306-1285delinsCTA
ENST00000505652.1:c.*169-1287_*169-1285delinsCTA ENSP00000421556.1:n.*169-1287_*169-1285delinsCTA
ENST00000508511.5:n.362-1287_362-1285delinsCTA
ENST00000512604.1:n.205-1287_205-1285delinsCTA
ENST00000512621.5:n.333-1287_333-1285delinsCTA
ENST00000512659.5:c.*32-1287_*32-1285delinsCTA ENSP00000424650.1:n.*32-1287_*32-1285delinsCTA
ENST00000512991.5:n.543-1287_543-1285delinsCTA
ENST00000626055.2:c.*32-1287_*32-1285delinsCTA ENSP00000487496.1:n.*32-1287_*32-1285delinsCTA
NM_000671.4:c.345-1287_345-1285delinsCTA MANE Select NP_000662.3:n.345-1287_345-1285delinsCTA